Osler-Weber-Rendu Syndrome - Dental Implications
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
18/04/2012
18/04/2012
2009
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Resumo |
Osler-Weber-Rendu syndrome (OWRS) is a rare hereditary, autosomal dominant disease characterized by a local angiodysplasia. Its clinical characteristics are vascular hamartomas of the skin and oral mucosa, arteriovenous malformations in the lungs, liver, kidney and brain, and episodes of epistaxis. The oral lesions, which become apparent through hemorrhagic telangiectasia, may be the first sign of the disease. This is a case report of a 74-year-old woman whose diagnosis of OWRS was established by her dentist based on the presence of telangiectasia in the skin and oral mucosa, reports of frequent nosebleeds of unknown etiology and a family history of telangiectasia. Amputation of a lower limb and comorbidities, such as cardiopathy, nephropathy and rheumatic disorders, completed the profile. OWRS causes major vascular changes that can be diagnosed initially by a dentist. In this article, we describe the skills and knowledge that dentists need to monitor patients with OWRS properly. |
Identificador |
JOURNAL OF THE CANADIAN DENTAL ASSOCIATION, v.75, n.7, p.527-530, 2009 1488-2159 |
Idioma(s) |
eng |
Publicador |
CANADIAN DENTAL ASSOC |
Relação |
Journal of the Canadian Dental Association |
Direitos |
openAccess Copyright CANADIAN DENTAL ASSOC |
Palavras-Chave | #HEREDITARY HEMORRHAGIC TELANGIECTASIA #PULMONARY ARTERIOVENOUS-MALFORMATIONS #BRAIN-ABSCESS #DISEASE #MANIFESTATIONS #UPDATE #Dentistry, Oral Surgery & Medicine |
Tipo |
article original article publishedVersion |